ClinVar Miner

Submissions for variant NM_004588.5(SCN2B):c.324C>T (p.Tyr108=)

gnomAD frequency: 0.00001  dbSNP: rs981151593
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001480979 SCV001685311 likely benign Atrial fibrillation, familial, 14 2020-07-16 criteria provided, single submitter clinical testing

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